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Synthesis
and Characterization of Hydroxyethylstarch Hydrogels as Drug Delivery
Systems
A successful application
of proteins as active ingredients depends on the availability of
an efficient delivery and release system, which allows a controlled
release of physiological amounts of proteins next to the target
tissue over a certain period of time. The approach to such a drug
delivery system is the entrapment of proteins in a hydrogel matrix.
With the ability of hydrogels to incorporate a huge amount of water
or buffer, they offer optimal conditions for long in vivo-lifetimes
of proteins. Our hydrogel delivery system bases on photocrosslinking
of hydroxyethylmethacrylate-hydroxy-ethylstarch (HESHEMA, Fig. 1)
in the presence of proteins (Fig. 2).

Fig.
1 HESHEMA

Fig.
2 Photocrosslinking
HES has been used
in medicine for a long time, so that the physiological compatibility
of the hydrogels can be assumed. Modifications in the Degree of
substitution of the crosslinkable HEMA-group afford hydrogels with
different mesh sizes. Furthermore this hydrogelmatrix is biodegradable,
so that a continuous release of active ingredients in the course
of the erosion of the hydrogel and diffusion is possible.
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